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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04027127
Other study ID # aksaray 2013-23
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 15, 2013
Est. completion date June 15, 2018

Study information

Verified date July 2019
Source Aksaray University Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In our study, Netrin -1; We found that patients with ACS increased at the time of admission, decreased TIMI 3 flow after angiography, and higher risk groups in high risk groups such as TIMI and GRACE were found to have higher Netrin-1 levels.


Recruitment information / eligibility

Status Completed
Enrollment 238
Est. completion date June 15, 2018
Est. primary completion date August 15, 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients over the age of 18

- diagnose ACS

- patients undergoing angiography

Exclusion Criteria:

- CVE history

- Neurological disease

- Pregnancy and Lactation

- Liver failure

- Diagnosed malignity

- Use of anticonvulsant and nephrotoxic medication

- Chronic kidney disease

- Not having angiography

- Developing acute renal failure after angiography

- Patients who rejected to participate were excluded.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
netrin-1 value on admission to hospital


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Aksaray University Training and Research Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary serum netrin-1 value Netrin-1 in plasma was measured by enzyme-linked immunosorbent assay (ELISA) (Mybiosource MBS044526 ) All assays were performed in duplicate. Plasma Netrin-1 is expressed in picograms (pg) per mg. 30 minute
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